Common heartburn meds may raise risks for liver patients, new study warns
NCT ID NCT06861478
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether giving proton pump inhibitors (like omeprazole) to people with cirrhosis who have bleeding in the esophagus causes more complications in the hospital. Researchers will randomly assign 60 adults to receive either the drug or no drug after an endoscopic procedure. They will track problems like confusion, infections, re-bleeding, shock, and kidney failure to see if the medication makes things worse.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2024
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Adult * Cirrhosis * Variceal Bleeding with only endoscopic findings consistent with portal hypertension complications * Hypovolemic shock and Variceal bleeding Exclusion Criteria: * Shock of any type other than hypovolemic. * No cirrhotic patients * Patients that have severe Hepatic Encephalopathy at admission (West Haven 3 and 4) * Hepatorenal syndrome * Acute on chronic with CLIF-C \>50 points * Septic patients * Spontaneous Bacterial Peritonitis Elimination Criteria * Voluntary removal of the study * Violation of the study protocol * Patients in the no PBI group that need prolonged mecánica ventilación.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Universitario "Jose E. González" de la Facultad de Medicina, Universidad Autónoma de Nuevo León
RECRUITINGMonterrey, Nuevo León, 64460, Mexico
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Other studies related to the condition(s) this trial covers.
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- Could a wearable zapper quiet cirrhosis pain without drugs?
- A needle through the gut could replace the standard liver pressure test
- Can two experimental drugs be used safely in people with cirrhosis?
- Can bedside ultrasound guide fluid treatment for cirrhosis patients?